Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Enrico Farnetti"'
Primary Vitreoretinal Lymphoma: Current Diagnostic Laboratory Tests and New Emerging Molecular Tools
Autor:
Beatrice Melli, Pietro Gentile, Davide Nicoli, Enrico Farnetti, Stefania Croci, Fabrizio Gozzi, Elena Bolletta, Luca De Simone, Francesca Sanguedolce, Andrea Palicelli, Maurizio Zizzo, Stefano Ricci, Fiorella Ilariucci, Cristiana Rossi, Alberto Cavazza, Stefano Ascani, Luca Cimino, Magda Zanelli
Publikováno v:
Current Oncology, Vol 29, Iss 10, Pp 6908-6921 (2022)
Primary vitreoretinal lymphoma (PVRL), a rare aggressive malignancy primarily involving the retina and/or the vitreous, is a major diagnostic challenge for clinicians (who commonly misdiagnose it as chronic uveitis) as well as for pathologists (for b
Externí odkaz:
https://doaj.org/article/d67278b362e5462aa0f23309b547f580
Autor:
Fabrizio Gozzi, Marco Bertolini, Pietro Gentile, Laura Verzellesi, Valeria Trojani, Luca De Simone, Elena Bolletta, Valentina Mastrofilippo, Enrico Farnetti, Davide Nicoli, Stefania Croci, Lucia Belloni, Alessandro Zerbini, Chantal Adani, Michele De Maria, Areti Kosmarikou, Marco Vecchi, Alessandro Invernizzi, Fiorella Ilariucci, Magda Zanelli, Mauro Iori, Luca Cimino
Publikováno v:
Diagnostics, Vol 13, Iss 14, p 2451 (2023)
Anterior segment optical coherence tomography (AS-OCT) allows the explore not only the anterior chamber but also the front part of the vitreous cavity. Our cross-sectional single-centre study investigated whether AS-OCT can distinguish between vitreo
Externí odkaz:
https://doaj.org/article/6ea7407fb1464dd28a9ef8b45c366d7e
Autor:
Aurelio Negro, Ignazio Verzicco, Stefano Tedeschi, Nicoletta Campanini, Magda Zanelli, Emanuele Negri, Enrico Farnetti, Davide Nicoli, Barbara Palladini, Rosaria Santi, Davide Cunzi, Anna Calvi, Pietro Coghi, Luigi Gerra, Riccardo Volpi, Gallia Graiani, Aderville Cabassi
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundPheochromocytoma (PHEO) clinical manifestations generally mirror excessive catecholamines secretion; rarely the clinical picture may reflect secretion of other hormones. Watery diarrhea, hypokalemia and achlorhydria (WDHA) is a rare syndrom
Externí odkaz:
https://doaj.org/article/d7490cad9d4841b69d751be593d1e136
Autor:
Andrea Palicelli, Stefania Croci, Alessandra Bisagni, Eleonora Zanetti, Dario De Biase, Beatrice Melli, Francesca Sanguedolce, Moira Ragazzi, Magda Zanelli, Alcides Chaux, Sofia Cañete-Portillo, Maria Paola Bonasoni, Stefano Ascani, Antonio De Leo, Guido Giordano, Matteo Landriscina, Giuseppe Carrieri, Luigi Cormio, Jatin Gandhi, Davide Nicoli, Enrico Farnetti, Simonetta Piana, Alessandro Tafuni, Martina Bonacini
Publikováno v:
Biomedicines, Vol 10, Iss 2, p 236 (2022)
Pembrolizumab (anti-PD-1) is allowed in selected metastatic castration-resistant prostate cancer (PC) patients showing microsatellite instability/mismatch repair system deficiency (MSI-H/dMMR). BRCA1/2 loss-of-function is linked to hereditary PCs and
Externí odkaz:
https://doaj.org/article/bbb5dfa57c564073ba1cde3a06351b4f
Autor:
Magda Zanelli, Stefano Ricci, Francesca Sanguedolce, Andrea Palicelli, Enrico Farnetti, Alessandro Tafuni, Maurizio Zizzo, Riccardo Valli, Maria Isabel Alvarez De Celis, Alberto Cavazza, Caterina Longo, Stefano Ascani
Publikováno v:
Life, Vol 11, Iss 10, p 1069 (2021)
Mycosis fungoides and nodal classic Hodgkin lymphoma (cHL) have been reported to occur concurrently or sequentially in the same patient. A long-lasting mycosis fungoides more often precedes the onset of nodal cHL, although few cases of nodal cHL foll
Externí odkaz:
https://doaj.org/article/37745ae24f454ad7bae0569f4595c0e6
Autor:
Fabiola Atzeni, Luigi Boiardi, Augusto Vaglio, Davide Nicoli, Enrico Farnetti, Alessandra Palmisano, Nicolò Pipitone, Davide Martorana, Gabriella Moroni, Selena Longhi, Francesco Bonatti, Carlo Buzio, Carlo Salvarani
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e62330 (2013)
OBJECTIVE: Chronic periaortitis (CP) is a rare disease that is characterised by fibro-inflammatory tissue surrounding the abdominal aorta and has both non-aneurysmal (idiopathic retroperitoneal fibrosis [IRF]) and aneurysmal forms (inflammatory abdom
Externí odkaz:
https://doaj.org/article/c89555f7100541c3a09c7e7c3f17fc5d
Autor:
Chiara Marraccini, Barbara Iotti, Petronilla Vanzanelli, Elisa Bedeschi, Enrico Farnetti, Davide Nicoli, Pamela Berni, Agnese Razzoli, Eleonora Maurizi, Gaia Gavioli, Angela Mazzi, Roberto Baricchi, Lucia Merolle, Davide Schiroli
Publikováno v:
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.
Several ABO gene mutations are known to determine rare subgroups: these ABO variants are often responsible for weak or null phenotypes and may cause an incorrect determination of the serotype. Here we describe for the first time the phenotypic discre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887bf10aff5fa2e00c2ee76863bb650a
https://pubmed.ncbi.nlm.nih.gov/36535828
https://pubmed.ncbi.nlm.nih.gov/36535828
Autor:
Elena Galli, Luigi Boiardi, Peter C. Grayson, Nicholas Balanda, Chiara Marvisi, Nicolò Pipitone, David B. Beck, Orsola Bonanno, Carlo Salvarani, Enrico Farnetti, Francesco Muratore, Davide Nicoli, Piera Zaldini, Paola Castrignanò, Rosina Longo
Publikováno v:
Arthritisrheumatology (Hoboken, N.J.). 74(4)
To identify patients with VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome) from a single-center cohort of Italian patients with vasculitis, using a clinically oriented phenotype-first approach.We retrospectively revi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52deb47e2fc28c8e5e572e22af4e8994
https://pubmed.ncbi.nlm.nih.gov/34611997
https://pubmed.ncbi.nlm.nih.gov/34611997
Autor:
Davide Nicoli, Carmine Pinto, Francesco Iachetta, Raffaella Zamponi, Lorenzo Tofani, Alessandra Romagnani, Bruno Casali, Angela Damato, Maria Banzi, Enrico Farnetti, Candida Bonelli
Publikováno v:
British Journal of Cancer
Background Deleterious polymorphisms in the gene encoding DPD (DPYD) may result in severe reduction of DPD enzymatic activity that causes life-threatening toxicities when the standard dose of fluorouracil is used. The best panel of single-nucleotide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e40c9615f8c1021eee5d9701428e8bd
https://doi.org/10.1038/s41416-019-0423-8
https://doi.org/10.1038/s41416-019-0423-8
Autor:
Davide Nicoli, Elena Pavlidis, Ilenia Maini, Carlotta Spagnoli, Carlo Fusco, Alessandro Iodice, Daniele Frattini, Grazia Gabriella Salerno, Enrico Farnetti
Publikováno v:
Journal of Pediatric Neurology. 17:149-152
Schwartz–Jampel syndrome type 1 (SJS1) is an autosomal recessive chondrodystrophic myotonia, linked to heparan sulfate proteoglycan 2 (HSPG2) variants. We describe a patient with typical features of SJS1, but not obesity. Clinical exome sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55dbb9ba460de02c06d538cd5ac4b13e
https://doi.org/10.1055/s-0038-1668163
https://doi.org/10.1055/s-0038-1668163